Activated non-graphitizable hard carbon using orange peel with mesoporous structure has been prepared by pyrolyzation at 700, 800, 900 °C using chemical activation method. The activated orange peel-derived hard carbon has been characterized for its mesoporous and disordered structure. TG-DSC gives the information for the changes about sample composition and thermal stability of the materials. Increasing the carbonization temperature for orange peel precursor using NaOH as activating agent, elevates the pore diameter, which thereby facilitating the insertion of Na+. Raman and X-ray diffraction confirms the presence of disordered carbon. The surface morphology of the material was analyzed by scanning eletron microsope and nitrogen ( N2) adsorption and desorption analysis give the morphology, mesopore size (3.374, 3.39 and 4 nm) and surace area (60.164, 58.99 and 54.327 m2/g) of the orange peel-derived hard carbon. Hence, this work strongly evidences that the biomass-derived hard carbon with good porosity and paves way of superior electrochemical performance for emerging sodium ion batteries.

The paper deals with a comparative study of equilibrium and kinetics of phenol adsorption from aqueous solutions by means of commercial activated carbons and semi-cokes, differing in the nature of feedstock, production technology and structural characteristics. The main adsorption parameters are calculated with the usage of Langmuir and Dubinin–Radushkevich equations. The change in the characteristics of the structure and state of the surface of semi-coke P2 as a result of modification is estimated. It was found that phenol adsorption kinetics is described by a pseudo-second-order model. The adsorption rate constants and the coefficient of external diffusion mass transfer are calculated. It is proved that phenol extraction from aqueous solutions presents a mixed-diffusion nature, and the process rate is limited by external mass transfer for 13 min for SKD-515 and 22 min for ABG. To increase the adsorption capacity, the oxidative modification of the semi-coke P2 was carried out. Considering the economic and technological aspects, ABG semi-coke is recognized as a promising sorbent for phenol extraction from aqueous media.

Novel eco-friendly adsorbents were prepared through pyrolysis and acid activation of raw almond leaf (RAL) to form almond leaf biochar (ALB) and chemically activated almond leaf biochar (CAL), respectively. The prepared adsorbents were characterized using TGA, FTIR, SEM–EDX, BET and XRD techniques and their physicochemical properties investigated. RAL, ALB and CAL were utilized for adsorption of BPB dye from aqueous solution using batch technique under optimum conditions. The optimum dye adsorbed by RAL, ALB and CAL were 92.83, 93.21 and 94.89%, respectively at pH 3, dye initial conc. (100 mg/L), adsorbent dose (0.04 g/25 mL), 60 min contact time and 301 K adsorption temperature. Although, Langmuir maximum monolayer adsorption capacities were found to be 365.36, 535.62 and 730.46 mg/g for RAL, ALB and CAL, respectively, but isotherm conformed to Freundlich model. Kinetic study confirmed suitability of pseudo-second-order model with rate constant 9.33 × 10–4, 9.91 × 10–4 and 12.60 × 10−4 g mg−1 min−1 for RAL, ALB and CAL, respectively. Negative values of thermodynamic parameters (ΔG and ΔH) established sequestration process to be spontaneous and exothermic. RAL, ALB and CAL were discovered to be highly efficient adsorbents that could be used in place of expensive commercial adsorbents.

The high level of lithium storage in synthetic porous carbons has necessitated the development of accurate models for estimating the specific capacity of carbon-based lithium-ion battery (LIB) anodes. To date, various models have been developed to estimate the storage capacity of lithium in carbonaceous materials. However, these models are complex and do not take into account the effect of porosity in their estimations. In this paper, a novel model is proposed to predict the specific capacity of porous carbon LIB anodes. For this purpose, a new factor is introduced, which is called normalized surface area. Considering this factor, the contribution of surface lithium storage can be added to the lithium stored in the bulk to have a better prediction. The novel model proposed in this study is able to estimate the lithium storage capacity of LIB anodes based on the porosity of porous carbons for the first time. Benefiting porosity value (specific surface area) makes the predictions quick, facile, and sensible for the scientists and experts designing LIBs using porous carbon anodes. The predicted capacities were compared with that of the literature reported by experimental works. The remarkable consistency of the measured and predicted capacities of the LIB anodes also confirms the validity of the approach and its reliability for further predictions.

Double-layer graphene nanoribbons promise potential application in nanoelectromechanical systems and optoelectronic devices, and knowledge about mechanical stability is a crucial parameter to flourish the application of these materials at the next generation of nanodevices. In this paper, molecular mechanics is utilized to investigate nonlinear buckling behavior, critical buckling stress, and lateral deflection of double-layered graphene nanoribbons under various configurations of stacking mode and chirality. The implicit arc-length iterative method (modified Riks method) with Ramm’s algorithm is utilized to analyze the nonlinear structural stability problem. The covalent bonds are modeled using three-dimensional beam elements in which elastic moduli are calculated based on molecular structural mechanics technique, and the interlayer van der Waals (vdW) interactions are modeled with nonlinear truss elements. An analytical expression for Young’s modulus of nonlinear truss elements is derived based on the Lennard–Jones potential function and implemented in numerical simulation with a UMAT subroutine based on FORTRAN code to capture the nonlinearity of the vdW interactions during the buckling analysis. The results indicate that the highest critical buckling stress and the minimum lateral deflection occur for armchair and zigzag chirality, both with AB stacking mode, respectively. Moreover, the critical buckling stress is found to be directly dependent on the mode shape number regardless of in-phase or anti-phase deflection direction of layers. Lateral deflection exhibits a similar trend with mode shape in anti-phase mode; however, it is decreasing by increasing mode shape number in in-phase mode.

This work reports utilization of apple leaves as a source of activated carbon. Activated carbon from apple leaves is prepared by two different methods, thermal activation where AC1 is obtained and chemical activation using H3PO4 and ZnCl2 where AC2 and AC3 are obtained, respectively. XRD analysis revealed that all types of prepared ACs have a semi-crystalline nature with a mean crystallite size of 13, 21.02, and 39.47 nm for AC1, AC2, and AC3, respectively. To identify the most suitable desorption temperature, the exothermic behavior was discovered for the three types of ACs by DSC. The exothermic onset temperatures are 340 °C, 200 °C, 400 °C, or AC1, AC2, and AC3, respectively. The point of zero charge for the three types of ACs is 8.6, 7.3, and 2.5 for AC1, AC2, and AC3, respectively. The BET surface area analysis data demonstrated that mesoporous structure was developed in AC1 and AC2, while a microporous structure was developed in AC3. Quantum chemical calculations for ACs is carried out using Density Functional Theory (DFT). Application of the prepared ACs in adsorption of basic dye C.I. base blue 47 is studied. The maximum removal efficiency was 65.1%, 96% and 99% for AC1, AC2, and AC3, respectively under the influence of different operating aspects. Adsorption data are modeled by Langmuir, Freundlich, and Temkin isotherms. The data revealed that adsorption of basic dye C.I. base blue 47 on AC1 follows Langmuir isotherm and adsorption on AC2 and AC3 follows Freundlich isotherm.

COVID-19와 같은 전염병 감염 시나리오 전반에 걸쳐 펩타이드 기반 치료법을 발견하고 설계하는 개발 시대의 추세는 보다 효율적이고 저렴한 치료 환경으로 발전할 수 있습니다. 결과적으로, 그들의 단백질 분해 약화는 천연 펩타이드 약물의 단점 중 하나입니다. 펩티도미메틱스는 이 단점을 해결하는 데 도움이 될 수 있습니다. 이 리뷰에서 펩타이드 및 펩타이드 기반 약물 발견은 숙주 안지 오텐신 전환 효소-2(ACE2) 수용체 및 바이러스 스파이크 (S)단백질의 연관성을 포함하는 중증 코로나바이러스 폐색전 증후군(SARS-CoV-2)의 주요 진입 기전 중 하나를 표적으로 요약했습니다. 또한, 펩타이드 기반의 새로운 치료법을 통해 COVID-19에 대해 연구된 단백질, 펩타이드 및 기타 가능한 조치의 이점을 다룹니다. 그리고 펩타이드 기반 약물 치료 환경의 개요는 진화적 관점, 구조적 특성, 작동 한계값 및 치료 영역에 대한 설명으로 구성된다